Microsatellite analysis of plasma DNA from patients with clear cell renal carcinoma

Cancer Research

Volumn 58, Issue 20, 1998, Pages 4728-4732

  Goessl, Carsten ^a,c   Heicappell, Rüdiger ^a   Münker, Ralf ^a   Anker, Philippe ^b   Stroun, Maurice ^b   Krause, Hans ^a   Müller, Markus ^a   Miller, Kurt ^a  

^a FREIE UNIVERSITÄT BERLIN   (Germany)

^b Pavillon des Isotopes   (Switzerland)

^c CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA; TUMOR MARKER;

ARTICLE; CHROMOSOME 3P; CLEAR CELL CARCINOMA; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; FEMALE; GENE LOCUS; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; KIDNEY CARCINOMA; MALE; MICROSATELLITE INSTABILITY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ADENOCARCINOMA, CLEAR CELL; AGED; CHROMOSOMES, HUMAN, PAIR 3; DNA, NEOPLASM; FEMALE; HUMANS; KIDNEY NEOPLASMS; LOSS OF HETEROZYGOSITY; MALE; MICROSATELLITE REPEATS; MIDDLE AGED;

EID: 0032532399     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (33)

1. Sidransky, D. Nucleic acid-based methods for the detection of cancer. Science (Washington DC), 278: 1054-1058, 1997.
2. Steiner, G., Schoenberg, M. P., Linn, J. F., Mao, L., and Sidransky, D. Detection of bladder cancer recurrence by microsatellite analysis of urine. Nat. Med., 3: 621-624, 1997.
3. Knudson, A. G. Hereditary cancer: two hits revisited. J. Cancer Res. Clin. Oncol., 122: 135-140, 1996.
4. Fearon, E. R., and Vogelstein, B. A genetic model for colorectal carcinogenesis. Cell, 61: 759-767, 1990.
5. Steiner, G., and Sidransky, D. Molecular differential diagnosis of renal carcinoma: from microscopes to microsatellites. Am. J. Pathol., 149: 1791-1795, 1996.
6. Druck, T., Kastury, K., Hadaczek, P., Podolski, J., Toloczko, A., Sikorski, A., Ohta, M., LaForgia, S., Lasota, J., McCue, P., Lubinski, J., and Huebner, K. Loss of heterozygosity at the familial RCC t(3;8) locus in most clear cell renal carcinomas. Cancer Res., 55: 5348-5353, 1995.
7. Wilhelm, M., Bugert, P., Kenck, C., Staehler, G., and Kovacs, G. Terminal deletion of chromosome 3p sequences in nonpapillary renal cell carcinomas: a breakpoint cluster between loci D3S1285 and D3S1603. Cancer Res., 55: 5383-5385, 1995.
8. Shridhar, V., Wang, L., Rosati, R., Paradee, W., Shridhar, R., Mullins, C., Sakr, W., Grignon, D., Miller, O. J., Sun, Q. C., Petros, J., and Smith, D. I. Frequent breakpoints in the region surrounding FRA3B in sporadic renal cell carcinomas. Oncogene, 14: 1269-1277, 1997.
9. Chudek, J., Wilhelm, M., Bugert, P., Herbers, J., and Kovacs, G. Detailed microsatellite analysis of chromosome 3p region in non-papillary renal cell carcinomas. Int. J. Cancer, 73: 225-229, 1997.
10. Gnarra, J. R., Tory, K., Weng, Y., Schmidt, L., Wie, M. H., Li, H., Latif, F., Liu, S., Chen, F., Duh, F-M., Lubensky, I., Duan, D. R., Florence, C., Pozzatti, R., Walther, M. M., Bander, N. H., Grossman, H. B., Brauch, H., Pomer, S., Brooks, J. D., Isaacs, W. B., Lerman, M. I., Zbar, B., and Linehan, W. M. Mutations of the VHL tumour suppressor gene in renal carcinoma. Nat. Genet., 7: 85-90, 1994.
11. Chen, X. Q., Stroun, M., Magnenat, J-L., Nicod, L. P., Kurt, A-M., Lyautey, J., Ledderey, C., and Anker, P. Microsatellite alterations in plasma DNA of small cell lung cancer patients. Nat. Med., 2: 1033-1035, 1996.
12. Nawroz, H., Koch, W., Anker, P., Stroun, M., and Sidransky, D. Microsatellite alterations in serum DNA of head and neck cancer patients. Nat. Med., 2: 1035-1037, 1996.
13. Anker, P., Lefort, F., Vasioukhin, V., Lyautey, J., Ledderey, C., Chen, X. Q., Stroun, M., Mulcahy, H. E., and Farthing, J. G. K-ras mutations are found in DNA extracted from the plasma of patients with colorectal cancer. Gastroenterology, 112: 1114-1120, 1997.
14. Sorenson, G. D., Pribish, D. M., Valone, F. H., Memoli, V. A., Bzik, D. J., and Yao, S. L. Soluble normal and mutated DNA sequences from single-copy genes in human blood. Cancer Epidemiol. Biomark. Prev., 3: 67-71, 1994.
15. Kopreski, M. S., Benko, F. A., Kwee, C., Leitzel, K. E., Eskander, E., Lipton, A., and Gocke, C. D. Detection of mutant K-ras DNA in plasma or serum of patients with colorectal cancer. Br. J. Cancer, 76: 1293-1299, 1997.
16. Gyapay, G., Morisette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. The 1993-94 Genethon human genetic linkage map. Nat. Genet., 7: 246-249, 1994.
17. Cawkwell L., Bell, S. M., Lewis, F. A., Dixon, M. F., Taylor, G. R., and Quirke, P. Rapid detection of allele loss in colorectal tumours using microsatellites and fluorescent DNA technology. Br. J. Cancer, 67: 1262-1267, 1993.
18. Wang, Y., Hung, S-C., Linn, J. F., Steiner, G., Glazer, A. N., Sidransky, D., and Mathies, R. A. Microsatellite-based cancer detection using capillary array electrophoresis and energy-transfer fluorescent primers. Electrophoresis, 18: 1742-1749, 1997.
19. Hermanek, P., and Schrott, K. M. Evaluation of the new tumor, nodes and metastases classification of renal cell carcinoma. J. Urol., 144: 238-241, 1990.
20. Gruis, N. A., Abeln, E. C. A., Bardoel, A. F. J., Devilee, P., Frants, R. R., and Cornelisse, C. J. PCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue. Br. J. Cancer, 68: 308-313, 1993.
21. Shapiro, B., Chakrabarty, M., Cohn, E. M., and Leon, S. A. Determination of circulating DNA levels in patients with benign or malignant gastrointestinal disease. Cancer (Phila.), 51: 2116-2120, 1983.
22. Hadaczek, P., Podolski, J., Toloczko, A., Kurzawski, G., Sikorski, A., Rabbitts, P., Huebner, K., and Lubinski, J. Losses at 3p common deletion sites in subtypes of kidney tumours: histopathological correlations. Virchows Archiv., 429: 37-42, 1996.
23. Anker, P., Stroun, M., and Maurice, P. A. Spontaneous release of DNA by human blood lymphocytes as shown in an in vitro system. Cancer Res., 35: 2375-2382, 1975.
24. Böhm, M., and Wieland, I. Analysis of tumour-specific alterations in native specimens by PCR: how to procure the tumour cells! Int. J. Oncol., 10: 131-139, 1997.
25. Emmert-Buck, M. R., Bonner, R. F., Smith, P. D., Chuaqui, R. F., Zhuang, Z., Goldstein, S. R., Weiss, R. A., and Liotta, L. A. Laser capture microdissection. Science (Washington DC), 274: 998-1001, 1996.
26. Macintosh, C. A., Stower, M., Reid, N., and Maitland, N. J. Precise microdissection of human prostate cancers reveals genotypic heterogeneity. Cancer Res., 58: 23-28, 1998.
27. Takahashi, A., Sasaki, H., Kim, S. J., Tobisu, K., Kakizoe, T., Tsukamoto, T., Kumamoto, Y., Sugimura, T., and Terada, M. Markedly increased amounts of messenger RNAs for vascular endothelial growth factor and placenta growth factor in renal cell carcinoma associated with angiogenesis. Cancer Res., 54: 4233-4237, 1994.
28. Berger, D. P., Herbstritt, L., Dengler, W. A., Marme, D., Mertelsmann, R., and Fiebig, H. H. Vascular endothelial growth factor (VEGF) mRNA expression in human tumor models of different histologies. Ann. Oncol., 6: 817-825, 1995.
29. Fishel, R., and Kolodner, R. D. Identification of mismatch repair genes and their role in the development of cancer. Curr. Opin. Genet. Dev., 5: 382-395, 1995.
30. Thibodeau, S. N., Bren, G., and Schaid, D. Microsatellite instability in cancer of the proximal colon. Science (Washington DC), 260: 812-816, 1993.
31. Cairns, P., Tokino, K., Eby, Y., and Sidransky, D. Localization of tumor suppressor loci on chromosome 9 in primary human renal cell carcinomas. Cancer Res., 55: 224-227, 1995.
32. Reiter, R. E., Anglard, P., Liu, S., Gnarra, J. R., and Linehan, W. M. Chromosome 17p deletions and p53 mutations in renal cell carcinoma. Cancer Res., 53: 3092-3097, 1993.
33. Mulcahy, H. E., Lyautey, J., Ledderey, C., Chen, X. Q., Anker, P., Alstead, E. M., Ballinger, A., Farthing, M. J. G., and Stroun, M. A prospective study of K-ras mutations in the plasma of pancreatic cancer patients. Clin. Cancer Res., 4: 271-275, 1998.